Evidence map›Paper›PMID 32895645›Full record

ArticleCytokine: X2020

Tocilizumab for severe COVID-19 related illness - A community academic medical center experience.

Kapil S Meleveedu, John Miskovsky, Joseph Meharg, Abd Abdelrahman, Richa Tandon, Ashley E Moody, Priscilla Dasilva, Gabrielle Masse, Jason LaPorte, Abdul Saied Calvino and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Cytokine: X, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 1 country.

Kapil S MeleveeduImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
John MiskovskyDepartment of Medicine, Roger Williams Medical Center, Providence, RI, USA.
Joseph MehargDepartment of Medicine, Roger Williams Medical Center, Providence, RI, USA.
Abd AbdelrahmanDepartment of Medicine, Roger Williams Medical Center, Providence, RI, USA.
Richa TandonDepartment of Medicine, Roger Williams Medical Center, Providence, RI, USA.
Ashley E MoodyImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Priscilla DasilvaImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Gabrielle MasseImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Jason LaPorteImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Abdul Saied CalvinoImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Greg AllenDepartment of Medicine, Roger Williams Medical Center, Providence, RI, USA.
Rabih El-BizriDepartment of Medicine, Roger Williams Medical Center, Providence, RI, USA.
Todd RobertsImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Vincent ArmenioImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Steven C KatzImmuno-oncology Institute, CharterCare Health Partners, Providence, RI, USA.
Roger Williams Medical Center · USHealthPartners · USProvidence College · USBoston University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-CoV-2 virus responsible for the COVID-19 pandemic can result in severe or fatal disease in a subset of infected patients. While the pathogenesis of severe COVID-19 disease has yet to be fully elucidated, an overexuberant and harmful immune response to the SARS-CoV-2 virus may be a pivotal aspect of critical illness in this patient population. The inflammatory cytokine, IL-6, has been found to be consistently elevated in severely ill COVID-19 patients, prompting speculation that IL-6 is an important driver of the pathologic process. The inappropriately elevated levels of inflammatory cytokines in COVID-19 patients is similar to cytokine release syndrome (CRS) observed in cell therapy patients. We sought to describe outcomes in a series of severely ill patients with COVID-19 CRS following treatment with anti-IL-6/IL-6-Receptor (anti-IL-6/IL-6-R) therapy, including tocilizumab or siltuximab. At our academic community medical center, we formed a multi-disciplinary committee for selecting severely ill COVID-19 patients for therapy with anti-IL-6 or IL-6-R agents. Key selection criteria included evidence of hyperinflammation, most notably elevated levels of C-reactive protein (CRP) and ferritin, and an increasing oxygen requirement. By the data cutoff point, we treated 31 patients with anti-IL-6/IL-6-R agents including 12 who had already been intubated. Overall, 27 (87%) patients are alive and 24 (77%) have been discharged from the hospital. Clinical responses to anti-IL-6/IL-6-R therapy were accompanied by significant decreases in temperature, oxygen requirement, CRP, IL-6, and IL-10 levels. Based on these data, we believe anti-IL-6/IL-6-R therapy can be effective in managing early CRS related to COVID-19 disease. Further study of anti-IL-6/IL-6-R therapy alone and in combination with other classes of therapeutics is warranted and trials are underway.

Indexed as

(ALC), Absolute Lymphocyte Count(anti-IL-6/IL-6-R), Anti-IL-6/IL-6-Receptor(ARDS), Acute respiratory distress syndrome(BMI), Body mass indexC-reactive protein(CRP), C-reactive protein(CRS), Cytokine release syndrome(DNR/DNI), Do not resuscitate/do not intubate(ECMO), Extracorporeal membrane oxygenation(ESR), Erythrocyte sedimentation rateIL-6Infectious disease(IRB), Institutional review board(LDH), Lactate dehydrogenase(NIV), Noninvasive ventilation(PaO2/FiO2), Arterial oxygen partial pressure/fraction of inspired oxygen(RT-PCR), Reverse-transcriptase polymerase-chain-reaction(RWMC), Roger Williams Medical CenterSARS-CoV-2(SITC), Society for Immunotherapy of Cancer(SpO2), Peripheral capillary oxygen saturation

Identifiers

PMID32895645
PMCPMC7467014
OpenAlexW3082632811

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.